VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES— 510(k) K020113

Name: FDA 510(k) clearance K020113
Creator: U.S. Food and Drug Administration
Published: 2002-05-17

Substantially Equivalent

Vector Research & Development

FDA 510(k) clearance K020113 for VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES, Substantially Equivalent on 2002-05-17. Applicant: Vector Research & Development. Device class: 2.

Clearance details

Applicant: Vector Research & Development
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2002-01-11
Decision date: 2002-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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